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Bromisovalum

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Identification
Molecular formula
C9H11BrN2NaO3
CAS number
49618-84-4
IUPAC name
sodium;5-(2-bromoallyl)-5-isopropyl-4,6-dioxo-1H-pyrimidin-2-olate
State
State

At room temperature, Bromisovalum is in a solid state. It is generally stable under recommended storage conditions.

Melting point (Celsius)
160.00
Melting point (Kelvin)
433.20
Boiling point (Celsius)
495.20
Boiling point (Kelvin)
768.30
General information
Molecular weight
250.09g/mol
Molar mass
250.0860g/mol
Density
1.5221g/cm3
Appearence

Bromisovalum appears as a white crystalline powder. It is mostly odorless and has a slightly bitter taste.

Comment on solubility

Solubility of Sodium; 5-(2-bromoallyl)-5-isopropyl-4,6-dioxo-1H-pyrimidin-2-olate

The solubility of sodium; 5-(2-bromoallyl)-5-isopropyl-4,6-dioxo-1H-pyrimidin-2-olate can be influenced by several key factors:

  • Polarity: The presence of polar functional groups typically enhances solubility in polar solvents like water.
  • Hydrogen bonding: The compound's structure may allow for hydrogen bonding with solvent molecules, which can further increase solubility.
  • Temperature: Solubility often increases with an increase in temperature; thus, the compound may have better solubility in warm solvents.
  • Concentration: The maximum amount of the compound that can dissolve depends on the concentration limits of the solvent.

Experimental data is essential to provide specific insights into solubility. Generally, compounds with similar characteristics exhibit either high or low solubility based on their functional groups:

  • High solubility: Compounds with multiple ionic or polar functional groups.
  • Low solubility: Compounds with large hydrophobic regions or extensive aromatic systems.

Understanding these principles can be vital when predicting the behavior of sodium; 5-(2-bromoallyl)-5-isopropyl-4,6-dioxo-1H-pyrimidin-2-olate in various solvent environments.

Interesting facts

Interesting Facts about Sodium 5-(2-bromoallyl)-5-isopropyl-4,6-dioxo-1H-pyrimidin-2-olate

This compound, a derivative of pyrimidine, highlights the fascinating interplay between structure and biological activity in organic chemistry. Here are some engaging points to consider:

  • Unique Structure: The presence of both bromo and isopropyl substituents adds to the complexity of the compound’s geometry, influencing its reactivity and interaction with biological systems.
  • Pharmaceutical Potential: Compounds that incorporate pyrimidine frameworks are often explored for their potential as pharmaceuticals. Their unique functionality can lead to the development of new therapeutic agents.
  • Bromine Chemistry: The inclusion of a bromo group can enhance the compound's reactivity, making it a valuable intermediate in various organic synthesis reactions, such as nucleophilic substitution.
  • Role of Sodium Salts: When in its sodium salt form, this compound can exhibit improved solubility and stability, which are crucial for its practical applications, especially in medicinal chemistry.
  • Biological Significance: Pyrimidine derivatives are well-known for their roles in biochemistry, particularly as constituents of nucleotides and nucleic acids, making this compound potentially important for research in genetic materials.

In summary, sodium 5-(2-bromoallyl)-5-isopropyl-4,6-dioxo-1H-pyrimidin-2-olate serves as a captivating example of how intricate organic compounds can bridge theoretical chemistry and practical applications. Its blend of structural features opens up numerous avenues for further exploration and potential innovative uses in science and medicine.